A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530737



Internal ID20904098
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3854105..3859748hg38UCSC Ensembl
chr19:3854103..3859746hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg385644
hg195644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18047596
Samples
Known GenesZFR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530737
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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